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HRID 31112作成日:2026年10月26日

Water → 3-Benzyloxy-4-hydroxybenzaldehyde

https://huagongshe.com/reaction/31112

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzyl ChlorideHCID 7503—
反応物3,4-DihydroxybenzaldehydeHCID 8768—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物3-Benzyloxy-4-hydroxybenzaldehydeHCID 11020635—

反応手順

Under atmosphere of argon, to a suspension of sodium hydride (63%, 57.1 g) in anhydrous N,N-dimethylformamide (540 ml) was added a solution of 3,4-dihydroxybenzaldehyde (103.5 g) in anhydrous N,N-dimethylformamide (500 ml) dropwise slowly under cooling with ice. The reaction mixture was stirred for 30 minutes at room temperature, and to the mixture was added benzyl chloride (104 ml) under cooling with ice and it was stirred for 15 hours at room temperature. To the mixture was added water under cooling with ice, and was concentrated under reduced pressure. The residue was diluted by water and it was washed by methylene chloride. The methylene chloride layer was extracted by a 1N aqueous solution of sodium hydroxide. Combined aqueous layers were acidified by 2M hydrochloric acid and it was extracted by ethyl acetate. The organic layer was washed by a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from chloroform to give the title compound (99.4 g) having the following physical data.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425567B2
出典データセットuspto-grants-2008_09
ORD IDord-569c2eeea7344c388f2fc4138da0f71c
出典メモuspto-grants-2008_09